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HRID 15174作成日:2026年10月27日

7-Bromo-2,3-dihydro-1-benzofuran-5-carbaldehyde → 5-Formyl-2,3-dihydro-1-benzofuran-7-carbonitrile

https://huagongshe.com/reaction/15174

反応式

関与物質

役割名称HCID仕込み量
反応物7-Bromo-2,3-dihydro-1-benzofuran-5-carbaldehydeHCID 18526182—
反応物HCID 178418546HCID 178418546—
溶媒DimethylacetamideHCID 31374—
生成物5-Formyl-2,3-dihydro-1-benzofuran-7-carbonitrileHCID 5748690261.4%

反応手順

To a solution of 7-bromo-2,3-dihydro-1-benzofuran-5-carbaldehyde (1.3 g, 4.7 mmol) in dimethylacetamide (2 mL) was added copper(I) cyanide (0.41 g g, 4.7 mmol). The reaction was refluxed for 18 h, and then concentrated under reduced pressure. The residue was washed well with warm ethyl acetate. The combined ethyl acetate layer were concentrated and dried. The crude product was purified by flash column chromatography (silica gel, 4:1 and 2:1 hexane:ethyl acetate gradient) to afford the desired product (0.5 g, 50%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732460B2
出典データセットuspto-grants-2010_06
ORD IDord-5cffa760ea3a42c59d941a8a79d59029
出典メモuspto-grants-2010_06